光催化
氮化碳
光催化分解水
材料科学
分解水
X射线光电子能谱
接受者
氧烷
轨道能级差
光化学
密度泛函理论
碳纤维
光谱学
化学工程
分子
计算化学
催化作用
化学
有机化学
工程类
复合材料
物理
复合数
量子力学
凝聚态物理
作者
Yabin Jiang,Chi Cao,Yueyang Tan,Qianwen Chen,Lei Zeng,Wensheng Yang,Zongzhao Sun,Limin Huang
标识
DOI:10.1016/j.jmst.2022.09.024
摘要
It is a prospective strategy to produce sustainable energy by photocatalytic overall water splitting (POWS). This work aims to develop a simple method for integrating a donor-acceptor system into polymeric carbon nitride (PCN) structure, which could accelerate the charge separation significantly. In the as-prepared photocatalyst (COCNT), carbon and oxygen were successfully incorporated into the framework of PCN, and the chemical environment of C and O was well probed by X-ray absorption near-edge structure (XANES) and X-ray photoelectron spectroscopy (XPS). It showed that the C-containing and O-containing segments of COCNT played the role of a donor, while the heptazine part played the role of an acceptor. In addition, Density-functional-theory (DFT) calculations confirmed the spatial split of the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) for promoting charge separation. Impressively, COCNT could efficiently split pure water to generate hydrogen and oxygen. And, the photocatalytic hydrogen evolution rate over COCNT (1550.9 µmol g–1 h–1) is about 17-fold higher than that of PCN. Finally, we proposed a possible photocatalytic mechanism to explain the above results.
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